Variant #0000329131 (NC_000022.10:g.50964913_50964916del, NC_000022.10(NM_001257988.1):c.929-6_929-3del (TYMP))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.50964913_50964916del
DNA change (hg38) g.50526484_50526487del
Published as TYMP(NM_001113755.2):c.929-6_929-3del (p.?)
ISCN -
DB-ID TYMP_000009
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-17 16:11:39 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ODF3B NM_001014440.3 -?/. - c.*3998_*4001del r.(=) p.(=)
TYMP NM_001257988.1 -?/. - c.929-6_929-3del r.spl? p.?
SCO2 NM_005138.2 -?/. - c.-1024_-1021del r.(?) p.(=)
NCAPH2 NM_152299.3 -?/. - c.*3109_*3112del r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.